Structure of trans-1,4-polybutadiene synthesized with a new catalyst system |
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Authors: | Evgueni Antipov Yuri Podolsky Nikolai Platé Manfred Stamm Erhard W. Fischer |
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Affiliation: | 1. Topchiev Institute of Petrochemical Synthesis Russian Academy of Sciences , Leninsky pr. 29, Moscow, 117912, Russia;2. Max Planck-Institut für Polymerforschung , Ackermannweg 10, Postfach 3148, Mainz, D-55128, Germany |
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Abstract: | Abstract The structure, phase composition, and temperature behavior of two trans-1,4-polybutadienes (TPBs) were studied by means of x-ray scattering and differential scanning calorimetry (DSC) techniques. The two samples examined were (1) PB synthesized using an immobilized titanium-magnesium catalyst and (2) a random copolymer based on PB prepared with a homogeneous vanadium-containing catalyst used as a reference material. It was found that the nascent structure of the first PB involves three phases: crystalline, mesomorphic (low-temperature form), and amorphous. In the vicinity of 65°C, a first-order phase transition occurs. The system becomes biphasic and contains the high-temperature form of the mesophase, as well as the amorphous phase, component. Above 165°C, the polymer melts to form a single-phase isotropic melt with a structure typical of liquids. The lateral dimension of crystallites reversibly changes at the crystal-mesophase transition. It is suggested that during annealing of the mesophase formed by cooling of the isotropic melt, the chains acquire an extended conformation. Loss of regularity of the structure of macromolecules of TPB causes a reduction of phase transition temperatures, an increase of the imperfection of the crystalline phase, and a contraction of the temperature range of existence of the mesophase. |
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Keywords: | polyamide 6/organoclay nanocomposites temperature‐modulated DSC melting kinetics Debye model polymorphic effects |
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